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Functional properties of ferroelectrics and their changes with time depend crucially on the defect structure. In particular, point defects and bias fields induced by defect dipoles modify the field hysteresis and play an important role in fatigue and aging. However, a full understanding on how order, agglomeration and strength of defect dipoles affect phase stability and functional properties is still lacking. To close these gaps in knowledge, we screen these parameters by ab initio based molecular dynamics simulations with the effective Hamiltonian method for the prototypical ferroelectric material (Ba,Sr)TiO₃. Our findings suggest that the active surface area of the defects, rather than the defect concentration is the decisive factor. For a fixed defect concentration, clustering reduces the active surface area and thus the defect-induced changes of phase stability and field hysteresis. Particularly planar agglomerates of defects appear as promising route for the material design as their impact on the field hysteresis can be controlled by the field direction and as their impact on the phase stability shows a cross-over with the strength of the defect dipoles. For this agglomeration, we show that the recoverable stored energy can outperform the response of pristine (Ba,Sr)TiO even in its paraelectric phase due to a pinched double-loop field hysteresis.